首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparative evaluation of the E test agar dilution and broth microdilution for testing susceptibilities of Helicobacter pylori strains to 20 antimicrobial agents.
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Comparative evaluation of the E test agar dilution and broth microdilution for testing susceptibilities of Helicobacter pylori strains to 20 antimicrobial agents.

机译:E测试琼脂稀释和肉汤微量稀释对幽门螺杆菌菌株对20种抗菌剂敏感性的比较评估。

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摘要

The Epsilometer test (E test; AB Biodisk, Solna, Sweden), a new quantitative technique for the determination of antimicrobial susceptibility, was compared to reference methods (agar dilution and broth microdilution) for the antimicrobial susceptibility testing of Helicobacter pylori. Seventy-one H. pylori strains isolated from patients with duodenal ulcers were tested against 20 antimicrobial agents. The E test and the agar dilution method were carried out on Mueller-Hinton agar; the broth microdilution method was performed with Mueller-Hinton broth. The E-test results showed excellent correlation with the agar dilution results, with 91.3 and 98.8% agreement within 1 and 2 log2 dilution steps, respectively, in a total of 1,350 tests. The correlation between the E-test results and the broth microdilution results was slightly higher, with 91.6 and 99.1% agreement within 1 and 2 log2 dilution steps, respectively, in a total of 1,317 tests. There were six major errors and two very major errors by the metronidazole E test compared to the results obtained by reference methods. Excellent agreement between E-test, agar dilution, and broth microdilution results was found for resistance to erythromycin (8%), clarithromycin (6%), and tetracycline (6%). Our results confirm that the E test is comparable to standardized methods for susceptibility testing. Therefore, the E test is a reliable and alternative method for testing H. pylori susceptibility to a wide range of antimicrobial agents in clinical practice.
机译:Epsilometer试验(E试验; AB Biodisk,瑞典索尔纳)是一种确定抗菌药物敏感性的新定量技术,与参考方法(琼脂稀释法和肉汤微量稀释法)用于幽门螺杆菌的抗菌药物敏感性试验相比较。从十二指肠溃疡患者中分离出的71株幽门螺杆菌菌株针对20种抗菌药物进行了测试。在Mueller-Hinton琼脂上进行E检验和琼脂稀释法;肉汤微稀释法用Mueller-Hinton肉汤进行。 E-检验结果显示与琼脂稀释结果具有极好的相关性,在总共1,350个检验中,在1和2 log2稀释步骤中分别达到91.3和98.8%的一致性。 E-检验结果与肉汤微量稀释结果之间的相关性略高,在总共1,317个检验中,在1和2 log2稀释步骤中分别达到91.6%和99.1%的一致性。与通过参考方法获得的结果相比,甲硝唑E检验有6个主要错误和2个非常重要的错误。对于红霉素(8%),克拉霉素(6%)和四环素(6%)的耐药性,E-检验,琼脂稀释和肉汤微量稀释结果之间具有极好的一致性。我们的结果证实,E检验可与药敏试验的标准方法媲美。因此,E测试是在临床实践中测试幽门螺杆菌对多种抗菌剂敏感性的可靠且替代的方法。

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